Canonical Allele Identifier: CA450448655

Gene: GCLC GCLC-AS1

Linked Data

• dbSNP Id: rs1388551628
• MyVariant Identifiers: chr6:g.53371699C>G (hg19) ; chr6:g.53506901C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.53506901C>G , CM000668.2:g.53506901C>G	GRCh38
NC_000006.11:g.53371699C>G , CM000668.1:g.53371699C>G	GRCh37
NC_000006.10:g.53479658C>G	NCBI36
NG_012071.1:g.43133G>C
NG_012071.2:g.43229G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513939.6:c.1083+12G>C (GCLC)	ENSP00000424211.2:n.1083+12G>C
ENST00000616923.5:c.1038+12G>C (GCLC)	ENSP00000482756.2:n.1038+12G>C
ENST00000643939.1:c.1203+12G>C (GCLC)	ENSP00000495686.1:n.1203+12G>C
ENST00000650454.1:c.1197+12G>C (GCLC) MANE Select	ENSP00000497574.1:n.1197+12G>C
ENST00000229416.10:c.1197+12G>C (GCLC)	ENSP00000229416.6:n.1197+12G>C
ENST00000504353.1:n.166+12G>C (GCLC)
ENST00000509541.5:n.1642+12G>C (GCLC)
ENST00000616923.4:c.1083+12G>C (GCLC)	ENSP00000482756.1:n.1083+12G>C
NM_001197115.1:c.1083+12G>C (GCLC)	NP_001184044.1:n.1083+12G>C
NM_001498.3:c.1197+12G>C (GCLC)	NP_001489.1:n.1197+12G>C
XR_926886.1:n.2249C>G (GCLC-AS1)
XR_926887.1:n.2243C>G (GCLC-AS1)
XR_926888.1:n.471C>G (GCLC-AS1)
XR_926889.1:n.440C>G (GCLC-AS1)
NM_001498.4:c.1197+12G>C (GCLC) MANE Select	NP_001489.1:n.1197+12G>C
XM_017010749.1:c.486+12G>C (GCLC)	XP_016866238.1:n.486+12G>C
XR_926886.2:n.575C>G (GCLC-AS1)
NM_001197115.2:c.1083+12G>C (GCLC)	NP_001184044.1:n.1083+12G>C